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Joni Turunen
Joni Turunen
Clinical lecturer, University of Helsinki
在 helsinki.fi 的电子邮件经过验证 - 首页
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FinnGen provides genetic insights from a well-phenotyped isolated population
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, KM Donner, ...
Nature 613 (7944), 508-518, 2023
15952023
FinnGen: Unique genetic insights from combining isolated population and national health register data
MI Kurki, J Karjalainen, P Palta, TP Sipilä, K Kristiansson, K Donner, ...
medrxiv, 2022.03. 03.22271360, 2022
4272022
Comprehensive Study of the Clinical Phenotype of Germline BAP1 Variant-Carrying Families Worldwide
S Walpole, AL Pritchard, CM Cebulla, R Pilarski, M Stautberg, ...
JNCI: Journal of the National Cancer Institute 110 (12), 1328-1341, 2018
2372018
Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q
T Paunio, J Ekelund, T Varilo, A Parker, I Hovatta, JA Turunen, K Rinard, ...
Human molecular genetics 10 (26), 3037-3048, 2001
1982001
Analysis of four neuroligin genes as candidates for autism
T Ylisaukko-oja, K Rehnström, M Auranen, R Vanhala, R Alen, E Kempas, ...
European Journal of Human Genetics 13 (12), 1285-1292, 2005
1972005
Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years
MK Andersen, V Lundgren, JA Turunen, C Forsblom, B Isomaa, PH Groop, ...
Diabetes care 33 (9), 2062-2064, 2010
1252010
RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility
CGS Palmer, JA Turunen, JS Sinsheimer, S Minassian, T Paunio, ...
The American Journal of Human Genetics 71 (6), 1312-1319, 2002
812002
The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland
JA Turunen, JO Peltonen, OPH Pietiläinen, W Hennah, A Loukola, ...
Schizophrenia research 91 (1-3), 27-36, 2007
732007
Mixture model clustering of phenotype features reveals evidence for association of DTNBP1 to a specific subtype of schizophrenia
J Wessman, T Paunio, A Tuulio-Henriksson, M Koivisto, T Partonen, ...
Biological psychiatry 66 (11), 990-996, 2009
642009
Mitochondrial aspartate/glutamate carrier SLC25A12 gene is associated with autism
JA Turunen, K Rehnström, H Kilpinen, M Kuokkanen, E Kempas, ...
Autism Research 1 (3), 189-192, 2008
542008
Further evidence for linkage of autosomal-dominant medullary cystic kidney disease on chromosome 1q21
M Auranen, S Ala-Mello, JA Turunen, I Järvelä
Kidney international 60 (4), 1225-1232, 2001
522001
Association analysis of the AIRE and insulin genes in Finnish type 1 diabetic patients
JA Turunen, M Wessman, C Forsblom, R Kilpikari, M Parkkonen, ...
Immunogenetics 58, 331-338, 2006
502006
Genetic risk factors associated with preeclampsia and hypertensive disorders of pregnancy
JS Tyrmi, T Kaartokallio, AI Lokki, T Jääskeläinen, E Kortelainen, ...
JAMA cardiology 8 (7), 674-683, 2023
492023
BAP1 germline mutations in Finnish patients with uveal melanoma
JA Turunen, S Markkinen, R Wilska, S Saarinen, V Raivio, M Täll, ...
Ophthalmology 123 (5), 1112-1117, 2016
492016
RHD maternal–fetal genotype incompatibility and schizophrenia: extending the MFG test to include multiple siblings and birth order
P Kraft, CGS Palmer, AJ Woodward, JA Turunen, S Minassian, T Paunio, ...
European journal of human genetics 12 (3), 192-198, 2004
492004
Association of AKT1 with verbal learning, verbal memory, and regional cortical gray matter density in twins
OPH Pietiläinen, T Paunio, A Loukola, A Tuulio‐Henriksson, T Kieseppä, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150 …, 2009
432009
Rare protein-altering variants in ANGPTL7 lower intraocular pressure and protect against glaucoma
Y Tanigawa, M Wainberg, J Karjalainen, T Kiiskinen, G Venkataraman, ...
PLoS Genetics 16 (5), e1008682, 2020
412020
Keratoendotheliitis fugax hereditaria: a novel cryopyrin-associated periodic syndrome caused by a mutation in the nucleotide-binding domain, leucine-rich repeat family, pyrin …
JA Turunen, J Wedenoja, P Repo, RS Järvinen, JE Jäntti, S Mörtenhumer, ...
American journal of ophthalmology 188, 41-50, 2018
412018
Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland
H Kilpinen, T Ylisaukko-oja, K Rehnström, E Gaál, JA Turunen, E Kempas, ...
Human molecular genetics 18 (15), 2912-2921, 2009
412009
Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample
P Soronen, K Silander, M Antila, OM Palo, A Tuulio-Henriksson, ...
Biological psychiatry 64 (5), 438-442, 2008
302008
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